Clinical Trial Details
— Status: Completed
Administrative data
| NCT number |
NCT04099407 |
| Other study ID # |
PROMETEO Study |
| Secondary ID |
|
| Status |
Completed |
| Phase |
Phase 2
|
| First received |
|
| Last updated |
|
| Start date |
August 1, 2019 |
| Est. completion date |
December 31, 2020 |
Study information
| Verified date |
April 2024 |
| Source |
Grupo Mexicano para el Estudios de las Enfermedades Hepaticas |
| Contact |
n/a |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Interventional
|
Clinical Trial Summary
Pirfenidone (PFD), an oral antifibrotic drug with anti-inflammatory and anti-oxidant
properties, has been granted marketing authorization by the European Medicine Agency and FDA,
for the treatment of idiopathic pulmonary fibrosis (IPF). However, few studies have focused
on its clinical utilization in patients with advanced hepatic fibrosis. Therefore,
Investigators aim to evaluate a prolonged-release PFD formulation (PR-PFD) plus standard of
care management on disease progression in patients with advanced liver fibrosis (ALF).
Methods: Patients with diverse chronic liver disease etiology (alcohol-related, hepatitis B
or C, autoimmune or fatty liver disease) will be screened with two non invasive liver
fibrosis methods (Fibroscan®) and Fibro Test®) and those with ALF (F3 or F4) will be treated
for at least 12 months with PR-PFD. Antifibrotic effects Will be assessed at 6 and 12 months;
variations greater than 30% in estimated fibrosis scores or 1 point on the METAVIR scale will
be considered clinically significant. PFD plasma levels, serum endothelin-1, IL6, TNFα and
TGFβ1, Quality of life and fatigue scales will be evaluated. Parametric and non parametric
statistics will be utilized and p values lower tan 5% will be considered clinically
significant.
Description:
The study will be conducted in compliance with International Standard good clinical practices
(GCPs) and the Declaration of Helsinki. The protocol was approved by local Institutional
Review Board and registered in clinical trials.gov.
Clinical and Laboratory Evaluation Blood counts and liver function tests (bilirubin, albumin,
prothrombin time expressed as international normalized ratio (INR), serum transaminases,
glucose, and creatinine) are measured at 12-week intervals. Patient's somatometric
measurements (height and body weight), vital signs, and frequency of adverse events (AE) are
recorded. Liver enzymes will be scored as stable, improving, or worsening.
Study End Points The primary efficacy endpoint is a reduction of fibrosis score by at least
30% either in Fibro Test units or kilo Pascals (kPa) according to hepatic elastography or a
reduction of 1 point on the METAVIR scale. Secondary efficacy endpoints include improvement
in alanine aminotranferase (ALT) and/or aspartate aminotransferase (AST), albumin, serum
concentrations of TGFbeta, IL-1 and IL-6 and endothelin, and Child-Pugh and MELD scores.
Worsening MELD is defined as switching from a lower-score to a higher-score and improving as
switching from a higher-score to a lower-score, where Group 1 was MELD ≤ 9, Group 2 10-19,
and Group 3 > 20.
Primary safety endpoints include clinical side effects, blood profile abnormalities, overall
survival, and pharmacokinetic (PK) findings. Secondary safety endpoints included quality of
life scores.
Evaluation and Classification of Fibrosis Outcomes Fibrosis-regression profile (FRP):
decreases >30% in FT score or 30% in kPa in liver stiffness measurement (LSM) or decreasing 1
point on the METAVIR score comparing baseline and M12 measurements.
Fibrosis-stabilization profile (FSP): stable FT results or kPa measurements (variations lower
than 30%) or METAVIR score.
Fibrosis-progression profile (FPP): increases greater than 30% in FT score or kPa or
increasing 1 point on METAVIR.
Specific Evaluation and Classification of Biochemical Outcomes Biochemical markers: Blood
parameters determined after overnight fasting include: albumin, prothrombin time, total
bilirubin, ALT, AST, Alkaline phosphatase (AP), and gamma-glutamyltransferase (GGT), measured
in fresh serum within 8h of collection on an automated biochemistry analyzer (Hitachi 917;
Roche Diagnostics).
alpha-2-macroglobulin (A2M), apolipoprotein-A1, and haptoglobin levels will be assayed by
nephelometry (Image; Beckman Coulter).
Fibro Test®: blinded Fibrotest measurements will be performed on fresh serum and according to
the recommended pre-analytic and analytic methods.
Hepatic elastography: Transient Elastography (TE) is performed according to published
recommendations using the Fibro-Scan® M probe. LSM is expressed in kPa. Only procedures with
at least 10 validated measurements, >60% success rate, and an interquartile range <30% of the
median will be considered reliable. Patients with ascites will be offered real time shear
wave elastography (Aixplorer, Supersonic Imagine).
Cytokines and pirfenidone: Serum concentrations of Interleukin 6 (IL-6), transforming growth
factor beta (TGF-β1), endothelin 1 (ET-1), and tumor necrosis factor alpha (TNF-α) will be
quantified by ELISA in an automated enzyme-linked immunosorbent assay (EIA) analyzer Coda
Microplate System (Bio-Rad Laboratories, Inc., Hercules, California, USA) and values
normalized against serum of healthy volunteers with normal liver function and LSM <5 kPa
(F0).
Evaluation of Safety Profile Monitoring for safety and toxicity will be performed throughout
the study. When necessary, appropriate medical intervention will be provided.
Quality of life assessment: All patients will fill out the Euro-Qol Index survey, including
the visual analog scale evaluation at baseline and at 12 months. Investigators incorporate
the nonutility-based Short Form-36v2 survey, which provides a detailed profile of
health-related quality of life.
Ethical considerations. The study will be conducted in accordance with the Declaration of
Helsinki and the E6 Good Clinical Practice Standards International Conference on
Harmonization (ICH).
Statistical Data Analysis: Investigators will be using the Statistical Package for the Social
Sciences (SPSS) Statistical software 6.12 for Windows. Descriptive statistics include mean,
standard deviation standard error. A paired or unpaired t Test will be used to compare means
before and after study medication administration. Values <5% will be considered significant.
Kaplan Meier survival analyses will include all patients on active study-medication treatment
despite duration of exposure. Sample size calculation was based on the following assumptions:
(1) mean expected baseline elastography score of 27.4 kPa, standard deviation of 15.7;
expected estimated-fibrosis reduction rate higher than 30% (delta); (4) alpha error of 1%;
(5) an accepted beta error of 10% (power = 90%); (6) two tails. The final number of patients
required to find a significant difference using the G power statistical program was 61
patients.
